GW679769 may affect liver enzymes that metabolize warfarin. This study is designed to test the extent of the GW679769 affect on Warfarin levels in humans.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
97
Casopitant will be available in the dose strength of 20,30 or 50 mg
Warfarin will be available in the dose strength of 5 mg
GSK Investigational Site
Gainesville, Florida, United States
GSK Investigational Site
Buffalo, New York, United States
Plasma levels of Warfarin at Period 1: Day 9 to 14, Period 2: Day 2 & 3 and Day 5 to 16.
Time frame: Period 1: Day 9 to 14, Period 2: Day 2 & 3 and Day 5 to 16.
Plasma levels of casopitant at Period 2: Day 2 & 3 and Day 5 to 16.
Time frame: Period 2: Day 2 & 3 and Day 5 to 16.
Clinical lab tests monitoring of International Normalized Ratio (INR) adverse events vital signs 12 lead ECGs liver function tests
Time frame: throughout the study
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